Hydrangeaceae |
Carpenteria |
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hydrangea family, mock-orange family |
California tree-anemone, tree anemone |
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Habit | Subshrubs, shrubs, trees, or vines [herbs], evergreen or deciduous. | Shrubs. | ||||||||||||||||||||||||||||||||||||
Stems | erect, ascending, or spreading. |
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Bark | exfoliating in grayish sheets or strips. |
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Branches | ascending or spreading; twigs with simple trichomes. |
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Leaves | usually opposite, sometimes whorled [alternate], simple; stipules absent; petiole present or absent; blade sometimes palmately lobed, margins entire, serrate, serrulate, dentate, denticulate, or crenate; venation pinnate or acrodromous (Fendlera, Fendlerella, Philadelphus, Whipplea). |
persistent, opposite; petiole present; blade lanceolate to narrowly elliptic or oblong, herbaceous to coriaceous, margins entire or obscurely denticulate, usually revolute, sometimes plane; venation pinnate. |
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Inflorescences | terminal or axillary, cymes, panicles, racemes, or corymbs, or flowers solitary. |
terminal or axillary, cymes, 3–9(–13)-flowered; peduncle present. |
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Pedicels | present. |
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Flowers | bisexual [unisexual], or sometimes marginal ones sterile, radially symmetric (bisexual ones) or bilaterally symmetric with enlarged petaloid sepals (sterile ones); perianth and androecium nearly hypogynous, perigynous, or epigynous; hypanthium completely adnate to ovary or adnate to ovary proximally, free distally; sepals 4–12, distinct or connate basally; petals 4–12, connate basally [entirely, then calyptrate]; nectary usually present, rarely absent; stamens 8–200, usually distinct, sometimes connate proximally, free; anthers dehiscing by longitudinal slits; pistil 1, 2–12-carpellate, ovary less than 1/2 inferior, 1/2 inferior, or completely inferior, 1–12-locular, placentation usually axile proximally, parietal distally, rarely strictly axile or parietal; ovules 1–50 per locule, anatropous; styles 1–12, distinct or connate proximally to most of length; stigmas (1–)2–12. |
bisexual; perianth and androecium nearly hypogynous; hypanthium adnate to ovary proximally, free distally, patelliform, not ribbed in fruit; sepals persistent, 5–7, spreading, ovate to ovate-lanceolate or triangular, sparsely to densely appressed-pubescent abaxially; petals 5–7(–8), imbricate, spreading to reflexed, white, ovate, round, or depressed-elliptic, base sessile or obscurely clawed, surfaces glabrous; stamens 150–200; filaments distinct, essentially terete, not noticeably tapered from base to apex, apex not 2-lobed; anthers depressed-ovate; pistil 5–7-carpellate, ovary nearly superior, 5–7-locular; placentation axile proximally, parietal distally; style persistent, 1. |
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Fruits | capsules [berries], dehiscence septicidal, loculicidal, interstylar, or intercostal. |
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Capsules | conic to depressed-spheric, corticate to coriaceous, dehiscence basipetally septicidal to near base of fruit, delayed apically by persistent style. |
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Seeds | 1–50 per locule, funicular appendage present (Fendlerella, Whipplea) or absent. |
50 per locule, brown or reddish brown, ellipsoid. |
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x | = 10. |
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Hydrangeaceae |
Carpenteria |
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Distribution | North America; Mexico; Central America; South America; Eurasia; Pacific Islands |
CA |
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Discussion | Genera 17, species ca. 240 (9 genera, 25 species in the flora). A. Cronquist (1981) placed Hydrangeaceae among a group of woody families traditionally allied with Saxifragaceae. Phylogenetic studies consistently place Hydrangeaceae in the Cornales and sister to Loasaceae (A. L. Hempel et al. 1995; D. E. Soltis et al. 1995; L. Hufford et al. 2001; Hufford 2004). Within Hydrangeaceae, the western North American genera Fendlera and Jamesia form a clade (subfam. Jamesioideae L. Hufford) that is sister to the rest of the family (subfam. Hydrangeoideae Burnett) (Hufford et al.; Hufford). Subfamily Hydrangeoideae comprises two tribes: Philadelpheae de Candolle ex Duby and Hydrangeeae de Candolle. North American genera in the former are Carpenteria, Deutzia, Fendlerella, Philadelphus, and Whipplea. A molecular phylogenetic study by Y. De Smet et al. (2015) clarified relationships within Hydrangeeae, found Hydrangea to be polyphyletic, and promoted adoption of a broader concept of Hydrangea that includes the eight other genera in the tribe. The two North American genera in the tribe, Decumaria and Hydrangea, are circumscribed here in their traditional senses. The Hydrangeaceae are well represented in the paleobotanical record dating back to the Upper Cretaceous but best represented in the Tertiary (L. Hufford 2004). Some genera are sources of popular introduced or native ornamentals, including Carpenteria, Deutzia, Hydrangea, and Philadelphus. Some ornamentals have become established outside of cultivation in the flora area. A few North American Hydrangeaceae have reputed medicinal (D. E. Moerman 1998) or toxicologic (G. E. Burrows and R. J. Tyrl 2001) properties. Trichomes in most Hydrangeaceae consist of a long, unicellular portion, often borne on a multicellular base. The unicellular portion often bears tubercles on its surface. Sometimes instead of tubercles, it bears long extensions, making the trichome appear branched or dendritic. Such trichomes are here referred to as branched. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Species 1. Phylogenetic analyses place Carpenteria as sister to Philadelphus (L. Hufford 1997; D. E. Soltis et al. 1995) or as a clade nested within a paraphyletic Philadelphus (Guo Y. L. et al. 2013). Androecium development in the two genera is unique in Hydrangeaceae (Hufford 1998). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 12, p. 462. | FNA vol. 12, p. 485. | ||||||||||||||||||||||||||||||||||||
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Name authority | Dumortier | Torrey: Proc. Amer. Assoc. Advancem. Sci. 4: 192. (1851) | ||||||||||||||||||||||||||||||||||||
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